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US7678470B2 - Reinforced matrix for molten carbonate fuel cell using porous aluminum support and method for preparing the molten carbonate fuel cell comprising the reinforced matrix - Google Patents

Reinforced matrix for molten carbonate fuel cell using porous aluminum support and method for preparing the molten carbonate fuel cell comprising the reinforced matrix Download PDF

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Publication number
US7678470B2
US7678470B2 US11/208,175 US20817505A US7678470B2 US 7678470 B2 US7678470 B2 US 7678470B2 US 20817505 A US20817505 A US 20817505A US 7678470 B2 US7678470 B2 US 7678470B2
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matrix
fuel cell
aluminum support
molten carbonate
carbonate fuel
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US20060204770A1 (en
Inventor
Sung Pil Yoon
Seong Ahn Hong
In Hwan Oh
Tae Hoon Lim
Suk-Woo Nam
Heung Yong Ha
Jonghee Han
Eun Ae Cho
Jaeyoung Lee
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Korea Institute of Science and Technology KIST
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Korea Institute of Science and Technology KIST
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Assigned to KOREA INSTITUTE OF SCIENCE AND TECHNOLOGY reassignment KOREA INSTITUTE OF SCIENCE AND TECHNOLOGY ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: CHO, EUN AE, HA, HEUNG YONG, HAN, JONGHEE, HONG, SEONG AHN, LEE, JAEYOUNG, LIM, TAE HOON, NAM, SUK-WOO, OH, IN HWAN, YOON, SUNG PIL
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    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00—Fuel cells; Manufacture thereof
    • H01M8/02—Details
    • H01M8/0289—Means for holding the electrolyte
    • H01M8/0295—Matrices for immobilising electrolyte melts
    • G—PHYSICS
    • G06—COMPUTING OR CALCULATING; COUNTING
    • G06F—ELECTRIC DIGITAL DATA PROCESSING
    • G06F3/00—Input arrangements for transferring data to be processed into a form capable of being handled by the computer; Output arrangements for transferring data from processing unit to output unit, e.g. interface arrangements
    • G06F3/01—Input arrangements or combined input and output arrangements for interaction between user and computer
    • G06F3/02—Input arrangements using manually operated switches, e.g. using keyboards or dials
    • G06F3/0202—Constructional details or processes of manufacture of the input device
    • G06F3/021—Arrangements integrating additional peripherals in a keyboard, e.g. card or barcode reader, optical scanner
    • G—PHYSICS
    • G06—COMPUTING OR CALCULATING; COUNTING
    • G06F—ELECTRIC DIGITAL DATA PROCESSING
    • G06F3/00—Input arrangements for transferring data to be processed into a form capable of being handled by the computer; Output arrangements for transferring data from processing unit to output unit, e.g. interface arrangements
    • G06F3/01—Input arrangements or combined input and output arrangements for interaction between user and computer
    • G06F3/03—Arrangements for converting the position or the displacement of a member into a coded form
    • G06F3/033—Pointing devices displaced or positioned by the user, e.g. mice, trackballs, pens or joysticks; Accessories therefor
    • G06F3/0354—Pointing devices displaced or positioned by the user, e.g. mice, trackballs, pens or joysticks; Accessories therefor with detection of 2D relative movements between the device, or an operating part thereof, and a plane or surface, e.g. 2D mice, trackballs, pens or pucks
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00—Fuel cells; Manufacture thereof
    • H01M8/14—Fuel cells with fused electrolytes
    • H01M8/141—Fuel cells with fused electrolytes the anode and the cathode being gas-permeable electrodes or electrode layers
    • H01M8/142—Fuel cells with fused electrolytes the anode and the cathode being gas-permeable electrodes or electrode layers with matrix-supported or semi-solid matrix-reinforced electrolyte
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/30—Hydrogen technology
    • Y02E60/50—Fuel cells
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
    • Y02P70/50—Manufacturing or production processes characterised by the final manufactured product
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/12—All metal or with adjacent metals
    • Y10T428/12014—All metal or with adjacent metals having metal particles
    • Y10T428/12153—Interconnected void structure [e.g., permeable, etc.]
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/12—All metal or with adjacent metals
    • Y10T428/12479—Porous [e.g., foamed, spongy, cracked, etc.]
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/12—All metal or with adjacent metals
    • Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
    • Y10T428/12736—Al-base component

Definitions

  • the present invention relates to a reinforced matrix for a molten carbonate fuel cell using a porous aluminum support and to a method for preparing the molten carbonate fuel cell comprising the reinforced matrix.
  • a matrix in a molten carbonate fuel cell serves to prevent a cross-over of a reaction gas, to provide a conduction channel of a CO 3 2 ⁇ ion with a molten carbonate impregnated in the porous structure of the matrix and to insulate a cathode and an anode electrically.
  • the matrix is not an element participating in an electrochemical reaction but serves just as a support for an electrolyte, a pore size, a porosity, a stability for the electrolyte and a mechanical strength are very important in the matrix.
  • fracture and crack of the matrix due to a difference between coefficients of thermal expansion of the matrix and of the electrolyte according to a thermal cycle, and a change of a micro structure due to a long time operation are main causes of a degradation of performance and a reduction of life of a unit cell.
  • the method using the alumina fibers is not suitable for a commercialization of the MCFC.
  • the object of the present invention is to provide a reinforced matrix for a molten carbonate fuel cell using a porous aluminum support and a method for preparing the molten carbonate fuel cell comprising the reinforced matrix, where the method is simple and economic contrary to the prior art which uses the alumina fibers and takes very high costs, and where the mass production of the matrix is easy, and where strength of the matrix can be increased effectively and therefore there is no worry about fracture or crack.
  • a reinforced matrix for a molten carbonate fuel cell comprising a porous aluminum support, and a lithium aluminate, which is tape-cast on the porous aluminum support.
  • the porous aluminum support is a reticulate aluminum support.
  • the porous aluminum support is an aluminum support having a three-dimensional network structure.
  • a method for preparing a molten carbonate fuel cell comprising steps of tape-casting a lithium aluminate on a porous aluminum support so as to prepare a reinforced matrix (S 1 ); making a unit cell or a stack of the unit cells using the reinforced matrix (S 2 ); and heat treating the unit cell or the stack so as to oxidize the aluminum in the support into the lithium aluminate (S 3 ).
  • the porous aluminum support is a reticulate aluminum support.
  • the porous aluminum support is an aluminum support having a three-dimensional network structure.
  • FIG. 1 is a schematic view showing a reinforced matrix for a molten carbonate fuel cell wherein lithium aluminate is tape-cast on a reticulate aluminum support according to the first example of the invention
  • FIG. 2 is a schematic view showing a reinforced matrix for a molten carbonate fuel cell wherein lithium aluminate is tape-cast on an aluminum support having a three-dimensional network structure according to the second example of the invention.
  • lithium aluminate is tape-cast on a porous aluminum support, preferably a reticulate aluminum support, and more preferably an aluminum support having a three-dimensional network structure, so that it is possible to increase a strength of a matrix highly while maintaining a porosity and a pore size of the matrix to a level equal to those of the prior matrix.
  • the support is made of inexpensive aluminum, it is possible to prepare the matrix economically.
  • a tape casting slurry was prepared with a composition of lithium aluminate powders 32%, PVB B76 binder 10.5%, plasticizer DBP 9%, disperant (Solsperse 9000) 0.5%, defoamer (DAPPO-348) 1.0%, ethanol solvent 47%, by weight percent.
  • sample powders, disperant and defoamer were primarily mixed in the ethanol solvent for 24 hours, and then the binder and plasticizer were added in the primarily mixed solution and then they were secondarily mixed for 6 days.
  • a reticulate aluminum support (300 mesh) (Example 1) or a aluminum support having a three-dimensional network structure (Example 2, an average size of pores is 1 mm) was placed on a Mylar film (glycol terephthalic acid polyester) having a thickness of 125 ⁇ m and a silicon resin coated on a surface thereof, and then lithium aluminate was tape-cast so that the film could have a thickness which is about 1.5 times as thick as that of the aluminum support.
  • a reinforced matrix as shown in FIGS. 1 and 2 .
  • FIG. 1 is a schematic view showing a reinforced matrix for a molten carbonate fuel cell wherein lithium aluminate is tape-cast on a reticulate aluminum support according to the first example of the invention.
  • a reinforced matrix 30 according to the first example of the invention comprises lithium aluminate 20 tape-cast on a reticulate aluminum support 10 .
  • Aluminum in the reticulate aluminum support 10 reacts with an electrolyte at an operating condition and thus becomes oxidized into lithium aluminate.
  • FIG. 2 is a schematic view showing a reinforced matrix for a molten carbonate fuel cell wherein lithium aluminate is tape-cast on an aluminum support having a three-dimensional network structure according to the second example of the invention.
  • a reinforced matrix 31 according to the second example of the invention comprises lithium aluminate 20 tape-cast on the aluminum support 11 having a three-dimensional network structure.
  • Aluminum in the aluminum support 11 having the three-dimensional network structure reacts with an electrolyte at an operating condition and thus becomes oxidized into lithium aluminate.
  • the matrixes (example 1 and example 2) reinforced with the reticulate aluminum support or the aluminum support having the three-dimensional network structure and a matrix reinforced with general alumina fibers (comparative example) were sintered under air atmosphere at 650° C., and then three-points bending strength test was performed for the respective matrixes.
  • the reinforced matrix prepared according to the first example exhibited about five times bending strength (0.5 Kgf/mm 2 ) compared to a bending strength (0.1 Kgf/mm 2 ) of the matrix having general alumina fibers added thereto.
  • the reinforced matrix prepared according to the second example exhibited about ten times bending strength (1.0 Kgf/mm 2 ) compared to the bending strength (0.1 Kgf/mm 2 ) of the matrix having general alumina fibers added thereto.
  • the method for preparing the matrix is simple, economic and suitable for a mass production.
  • the cost for the method is inexpensive since the support is made of inexpensive aluminum.
  • the aluminum reacts with the electrolyte when heat-treating of a unit cell or a stack of the unit cells comprising the matrix and thus becomes oxidized into lithium aluminate, it is possible to make a overall material of the reinforced matrix be equal and thus to minimize a strength reduction of the matrix due to corrosion or a difference between the coefficients of thermal expansion.

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  • Sustainable Energy (AREA)
  • Sustainable Development (AREA)
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  • Electrochemistry (AREA)
  • Theoretical Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Manufacturing & Machinery (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Engineering & Computer Science (AREA)
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Abstract

Disclosed is a reinforced matrix for a molten carbonate fuel cell comprising a porous aluminum support and a lithium aluminate tape-cast on the porous aluminum support. Further, disclosed is a method for preparing the molten carbonate fuel cell comprising the reinforced matrix comprising steps of tape-casting a lithium aluminate on a porous aluminum support so as to prepare a reinforced matrix (S1), making a unit cell or a stack of the unit cells using the reinforced matrix (S2) and heat treating the unit cell or the stack so as to oxidize aluminum in the support into lithium aluminate (S3). According to the present invention, the method is simple and economic, and the mass production of the matrix is easy, and strength of the matrix can be increased effectively and therefore there is no worry about fracture or crack.

Description

BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention relates to a reinforced matrix for a molten carbonate fuel cell using a porous aluminum support and to a method for preparing the molten carbonate fuel cell comprising the reinforced matrix.
2. Description of the Related Art
A matrix in a molten carbonate fuel cell (MCFC) serves to prevent a cross-over of a reaction gas, to provide a conduction channel of a CO3 2− ion with a molten carbonate impregnated in the porous structure of the matrix and to insulate a cathode and an anode electrically.
Since the matrix is not an element participating in an electrochemical reaction but serves just as a support for an electrolyte, a pore size, a porosity, a stability for the electrolyte and a mechanical strength are very important in the matrix.
In particular, fracture and crack of the matrix due to a difference between coefficients of thermal expansion of the matrix and of the electrolyte according to a thermal cycle, and a change of a micro structure due to a long time operation are main causes of a degradation of performance and a reduction of life of a unit cell.
To solve the above problems, there have been suggested methods of dispersing a secondary phase of ceramic fibers or coarse particles as a retardant of crack propagation in γ-LiAlO2 matrix to reinforce the matrix. As a result, it is known that an addition of alumina fibers is relatively efficient for reinforcing the matrix.
However, it is very expensive to manufacture the matrix using the alumina fibers. In view of that, the method using the alumina fibers is not suitable for a commercialization of the MCFC.
SUMMARY OF THE INVENTION
Accordingly, the present invention has been made to solve the above-mentioned problems occurring in the prior art. The object of the present invention is to provide a reinforced matrix for a molten carbonate fuel cell using a porous aluminum support and a method for preparing the molten carbonate fuel cell comprising the reinforced matrix, where the method is simple and economic contrary to the prior art which uses the alumina fibers and takes very high costs, and where the mass production of the matrix is easy, and where strength of the matrix can be increased effectively and therefore there is no worry about fracture or crack.
In order to accomplish the object, there is provided a reinforced matrix for a molten carbonate fuel cell comprising a porous aluminum support, and a lithium aluminate, which is tape-cast on the porous aluminum support.
In the reinforced matrix for a molten carbonate fuel cell according to the present invention, the porous aluminum support is a reticulate aluminum support.
In the reinforced matrix for a molten carbonate fuel cell according to the present invention, the porous aluminum support is an aluminum support having a three-dimensional network structure.
In order to achieve the above object, there is provided a method for preparing a molten carbonate fuel cell comprising steps of tape-casting a lithium aluminate on a porous aluminum support so as to prepare a reinforced matrix (S1); making a unit cell or a stack of the unit cells using the reinforced matrix (S2); and heat treating the unit cell or the stack so as to oxidize the aluminum in the support into the lithium aluminate (S3).
In the method according to the present invention, the porous aluminum support is a reticulate aluminum support.
In the method according to the present invention, the porous aluminum support is an aluminum support having a three-dimensional network structure.
BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 is a schematic view showing a reinforced matrix for a molten carbonate fuel cell wherein lithium aluminate is tape-cast on a reticulate aluminum support according to the first example of the invention; and
FIG. 2 is a schematic view showing a reinforced matrix for a molten carbonate fuel cell wherein lithium aluminate is tape-cast on an aluminum support having a three-dimensional network structure according to the second example of the invention.
 DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
Hereinafter, the present invention will be described in detail with reference to the accompanying drawings.
According to the invention, lithium aluminate is tape-cast on a porous aluminum support, preferably a reticulate aluminum support, and more preferably an aluminum support having a three-dimensional network structure, so that it is possible to increase a strength of a matrix highly while maintaining a porosity and a pore size of the matrix to a level equal to those of the prior matrix.
In addition, since the support is made of inexpensive aluminum, it is possible to prepare the matrix economically.
Also, since it is possible to react the aluminum in the matrix with an electrolyte and thus to in-situ oxidize the aluminum into lithium aluminate by heat-treating a unit cell or a stack of the unit cells comprising the matrix, it is possible to make a overall material of the reinforced matrix be equal and thus to minimize a strength reduction of the matrix due to corrosion or a difference between the coefficients of thermal expansion.
EXAMPLE
Preparation
A tape casting slurry was prepared with a composition of lithium aluminate powders 32%, PVB B76 binder 10.5%, plasticizer DBP 9%, disperant (Solsperse 9000) 0.5%, defoamer (DAPPO-348) 1.0%, ethanol solvent 47%, by weight percent.
The sample powders, disperant and defoamer were primarily mixed in the ethanol solvent for 24 hours, and then the binder and plasticizer were added in the primarily mixed solution and then they were secondarily mixed for 6 days.
In the prepared slurry, pores inevitably formed by air to be introduced in a milling process and solvent vapors to be generated due to the vapor pressure of the solvent. Accordingly, in order to prevent the generation of the pores, de-airing from the slurry solution was preformed using a rotary evaporator. Further, the de-airing was performed so that the viscosity of the slurry became 5,000˜10,000 cP, which is suitable for a tape-casting process.
A reticulate aluminum support (300 mesh) (Example 1) or a aluminum support having a three-dimensional network structure (Example 2, an average size of pores is 1 mm) was placed on a Mylar film (glycol terephthalic acid polyester) having a thickness of 125 μm and a silicon resin coated on a surface thereof, and then lithium aluminate was tape-cast so that the film could have a thickness which is about 1.5 times as thick as that of the aluminum support. As a result, obtained a reinforced matrix as shown in FIGS. 1 and 2.
FIG. 1 is a schematic view showing a reinforced matrix for a molten carbonate fuel cell wherein lithium aluminate is tape-cast on a reticulate aluminum support according to the first example of the invention.
As shown in FIG. 1, a reinforced matrix 30 according to the first example of the invention comprises lithium aluminate 20 tape-cast on a reticulate aluminum support 10. Aluminum in the reticulate aluminum support 10 reacts with an electrolyte at an operating condition and thus becomes oxidized into lithium aluminate.
FIG. 2 is a schematic view showing a reinforced matrix for a molten carbonate fuel cell wherein lithium aluminate is tape-cast on an aluminum support having a three-dimensional network structure according to the second example of the invention.
As shown in FIG. 2, a reinforced matrix 31 according to the second example of the invention comprises lithium aluminate 20 tape-cast on the aluminum support 11 having a three-dimensional network structure. Aluminum in the aluminum support 11 having the three-dimensional network structure reacts with an electrolyte at an operating condition and thus becomes oxidized into lithium aluminate.
Measurements and Results
The matrixes (example 1 and example 2) reinforced with the reticulate aluminum support or the aluminum support having the three-dimensional network structure and a matrix reinforced with general alumina fibers (comparative example) were sintered under air atmosphere at 650° C., and then three-points bending strength test was performed for the respective matrixes.
The reinforced matrix prepared according to the first example exhibited about five times bending strength (0.5 Kgf/mm2) compared to a bending strength (0.1 Kgf/mm2) of the matrix having general alumina fibers added thereto.
The reinforced matrix prepared according to the second example exhibited about ten times bending strength (1.0 Kgf/mm2) compared to the bending strength (0.1 Kgf/mm2) of the matrix having general alumina fibers added thereto.
As described above, according to the invention, it is possible to efficiently reinforce a matrix for a molten carbonate fuel cell. In addition, the method for preparing the matrix is simple, economic and suitable for a mass production. In particular, it is possible to increase the bending strength to about 10 times or more compared to that of the prior matrix while maintaining the porosity and the pore size to be equal to those of the prior matrix. In addition, the cost for the method is inexpensive since the support is made of inexpensive aluminum. Further, since the aluminum reacts with the electrolyte when heat-treating of a unit cell or a stack of the unit cells comprising the matrix and thus becomes oxidized into lithium aluminate, it is possible to make a overall material of the reinforced matrix be equal and thus to minimize a strength reduction of the matrix due to corrosion or a difference between the coefficients of thermal expansion.
Many alterations and modifications may be made by those having ordinary skill in the art without departing from the spirit and scope of the invention. Therefore, it must be understood that the embodiment and example described above should not be taken as limiting the invention as defined by the following claims. The claims are thus to be understood to include what is specifically described above, what is conceptionally equivalent, what can be obviously substituted and also what essentially incorporates the essential idea of he invention.

Claims (4)

1. A reinforced matrix for a molten carbonate fuel cell comprising:
a porous reticulate aluminum support consisting of aluminum; and
a lithium aluminate, which is tape-cast on the porous support.
2. The reinforced matrix according to claim 1, wherein the porous reticulate aluminum support is a 300 mesh porous reticulate aluminum support.
3. A reinforced matrix for a molten carbonate fuel cell comprising:
a porous aluminum support having a three dimensional network structure and consisting of aluminum; and
a lithium aluminate, which is tape-cast on the porous support.
4. The reinforced matrix according to claim 3, wherein the porous aluminum support is a porous aluminum support having a three-dimensional network structure, where an average pore size of the porous aluminum support is 1 mm.
US11/208,175 2005-03-14 2005-08-19 Reinforced matrix for molten carbonate fuel cell using porous aluminum support and method for preparing the molten carbonate fuel cell comprising the reinforced matrix Active 2027-10-28 US7678470B2 (en)

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US8637428B1 (en) 2009-12-18 2014-01-28 Simbol Inc. Lithium extraction composition and method of preparation thereof
US9034295B2 (en) 2009-04-24 2015-05-19 Simbol, Inc. Preparation of lithium carbonate from lithium chloride containing brines
US9034294B1 (en) 2009-04-24 2015-05-19 Simbol, Inc. Preparation of lithium carbonate from lithium chloride containing brines
US9051827B1 (en) 2009-09-02 2015-06-09 Simbol Mining Corporation Selective removal of silica from silica containing brines
US9074265B2 (en) 2010-02-17 2015-07-07 Simbol, Inc. Processes for preparing highly pure lithium carbonate and other highly pure lithium containing compounds
WO2015112982A1 (en) * 2014-01-27 2015-07-30 Fuelcell Energy, Inc. Fuel cell matrix composition and method of manufacturing same
US10604414B2 (en) 2017-06-15 2020-03-31 Energysource Minerals Llc System and process for recovery of lithium from a geothermal brine
US10829676B2 (en) 2009-04-24 2020-11-10 Terralithium Llc Treated geothermal brine compositions with reduced concentration of silica, iron and lithium
US11205795B2 (en) 2016-11-21 2021-12-21 Fuelcell Energy, Inc. Reinforced matrix for molten carbonate fuel cell and method for manufacturing the same
US11431016B2 (en) 2017-04-12 2022-08-30 Fuelcell Energy, Inc. Binder for electrolyte matrix for molten carbonate fuel cells
US11828272B2 (en) 2009-06-24 2023-11-28 Terralithium Llc Process for producing geothermal power, selective removal of silica and iron from brines, and improved injectivity of treated brines
US11904297B1 (en) 2023-01-11 2024-02-20 Iliad Ip Company, Llc Process for manufacturing lithium selective adsorption/separation media
US12168748B2 (en) 2009-04-24 2024-12-17 Terralithium Llc Treated geothermal brine compositions with reduced concentration of silica, iron and lithium
US12221671B2 (en) 2009-06-24 2025-02-11 Terralithium Llc Treated geothermal brine compositions with reduced concentrations of silica, iron and manganese

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KR20100047703A (en) 2008-10-29 2010-05-10 두산중공업 주식회사 An electrolyte-filled and reinforced matrix for molten carbonate fuel cell and method for producing the same
KR100980205B1 (en) * 2008-12-30 2010-09-03 두산중공업 주식회사 Method for manufacturing anode reinforcing sheet for in-situ sintering of molten carbonate fuel cell
KR101251374B1 (en) 2011-01-31 2013-04-05 한국과학기술연구원 Molten carbonate fuel cells including reinforced lithium aluminate matrix, method for preparing the same, and method of supplying lithium source

Citations (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4251600A (en) * 1979-12-27 1981-02-17 The United States Of America As Represented By The Department Of Energy Method of preparing a sintered lithium aluminate structure for containing electrolyte
JPS6124164A (en) * 1984-07-13 1986-02-01 Mitsubishi Electric Corp Electrolyte supporter of fused carbonate type fuel cell
JPS6386362A (en) * 1986-09-30 1988-04-16 Toshiba Corp Molten carbonate fuel cell stack
US4992341A (en) * 1988-10-21 1991-02-12 The United States Of America As Represented By The United States Department Of Energy Fabrication of dual porosity electrode structure
JPH0356631A (en) * 1989-07-25 1991-03-12 Mitsubishi Materials Corp Production of sintered plate of porous cu alloy for anode electrode of fused carbonate type fuel cell
US5354627A (en) * 1992-08-13 1994-10-11 Matsushita Electric Industrial Co., Ltd. Molten carbonate fuel cell
US5478663A (en) * 1994-03-22 1995-12-26 International Fuel Cells Corporation Edge seals for molten carbonate fuel cell stacks
US5589287A (en) * 1993-10-18 1996-12-31 Matsushita Electric Industrial Co., Ltd. Molten carbonate fuel cell
US5869203A (en) * 1996-12-13 1999-02-09 Energy Research Corporation Electrolyte matrix for molten carbonate fuel cells
US6153257A (en) * 1996-08-31 2000-11-28 Korea Institute Of Science And Technology Process for preparing a cathode containing alkaline earth metal oxides for molten carbonate fuel cells
US6290928B1 (en) * 1997-04-07 2001-09-18 Nippon Chemicals Industrial Co. Gamma lithium aluminate product and process of making
US6296972B1 (en) * 1998-04-24 2001-10-02 Korea Institute Of Science And Technology Method for preparing LICOO2-coated NiO cathodes for molten carbon fuel cell
US20010053475A1 (en) * 1998-12-17 2001-12-20 Qicong Ying Protective coating for separators for electrochemical cells
US6340454B1 (en) * 1998-12-28 2002-01-22 Nippon Chemical Industries Co., Ltd. α-Lithium aluminate and method of manufacturing the same, and electrolyte support material of molten carbonate fuel cell
US20040146736A1 (en) * 2003-01-29 2004-07-29 Advanced Materials Products, Inc. High-strength metal aluminide-containing matrix composites and methods of manufacture the same
US6824913B2 (en) * 2001-11-01 2004-11-30 Korea Institute Of Science And Technology Anode for molten carbonate fuel cell coated with porous ceramic films
US20060257722A1 (en) * 2005-05-16 2006-11-16 Abdelkader Hilmi High-lithium electrolyte for use in molten carbonate fuel cells and method for making same

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0509424A2 (en) 1991-04-16 1992-10-21 Institute of Gas Technology Composite active electrolyte-matrix and laminated component tapes for molten carbonate fuel cells
US5240786A (en) * 1992-03-13 1993-08-31 Institute Of Gas Technology Laminated fuel cell components
US5316555A (en) * 1992-11-03 1994-05-31 Institute Of Gas Technology Molten carbonate fuel cell electrolyte toughening
JPH0935730A (en) * 1995-07-14 1997-02-07 Toshiba Corp Molten carbonate fuel cell electrolyte matrix sheet and method for producing the same
JPH09129249A (en) * 1995-10-31 1997-05-16 Toshiba Corp Molten carbonate fuel cell
KR100368561B1 (en) * 1997-12-20 2003-03-28 한국전력공사 Method for Manufacturing Electrolyte Plate of Molten Carbonate Fuel Cells

Patent Citations (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4251600A (en) * 1979-12-27 1981-02-17 The United States Of America As Represented By The Department Of Energy Method of preparing a sintered lithium aluminate structure for containing electrolyte
JPS6124164A (en) * 1984-07-13 1986-02-01 Mitsubishi Electric Corp Electrolyte supporter of fused carbonate type fuel cell
JPS6386362A (en) * 1986-09-30 1988-04-16 Toshiba Corp Molten carbonate fuel cell stack
US4992341A (en) * 1988-10-21 1991-02-12 The United States Of America As Represented By The United States Department Of Energy Fabrication of dual porosity electrode structure
JPH0356631A (en) * 1989-07-25 1991-03-12 Mitsubishi Materials Corp Production of sintered plate of porous cu alloy for anode electrode of fused carbonate type fuel cell
US5354627A (en) * 1992-08-13 1994-10-11 Matsushita Electric Industrial Co., Ltd. Molten carbonate fuel cell
US5589287A (en) * 1993-10-18 1996-12-31 Matsushita Electric Industrial Co., Ltd. Molten carbonate fuel cell
US5478663A (en) * 1994-03-22 1995-12-26 International Fuel Cells Corporation Edge seals for molten carbonate fuel cell stacks
US6153257A (en) * 1996-08-31 2000-11-28 Korea Institute Of Science And Technology Process for preparing a cathode containing alkaline earth metal oxides for molten carbonate fuel cells
US5869203A (en) * 1996-12-13 1999-02-09 Energy Research Corporation Electrolyte matrix for molten carbonate fuel cells
US6290928B1 (en) * 1997-04-07 2001-09-18 Nippon Chemicals Industrial Co. Gamma lithium aluminate product and process of making
US6296972B1 (en) * 1998-04-24 2001-10-02 Korea Institute Of Science And Technology Method for preparing LICOO2-coated NiO cathodes for molten carbon fuel cell
US20010053475A1 (en) * 1998-12-17 2001-12-20 Qicong Ying Protective coating for separators for electrochemical cells
US6340454B1 (en) * 1998-12-28 2002-01-22 Nippon Chemical Industries Co., Ltd. α-Lithium aluminate and method of manufacturing the same, and electrolyte support material of molten carbonate fuel cell
US6824913B2 (en) * 2001-11-01 2004-11-30 Korea Institute Of Science And Technology Anode for molten carbonate fuel cell coated with porous ceramic films
US20040146736A1 (en) * 2003-01-29 2004-07-29 Advanced Materials Products, Inc. High-strength metal aluminide-containing matrix composites and methods of manufacture the same
US20060257722A1 (en) * 2005-05-16 2006-11-16 Abdelkader Hilmi High-lithium electrolyte for use in molten carbonate fuel cells and method for making same

Cited By (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US12252409B2 (en) 2009-04-24 2025-03-18 Terralithium Llc Preparation of lithium carbonate from lithium chloride containing brines
US12168748B2 (en) 2009-04-24 2024-12-17 Terralithium Llc Treated geothermal brine compositions with reduced concentration of silica, iron and lithium
US9034295B2 (en) 2009-04-24 2015-05-19 Simbol, Inc. Preparation of lithium carbonate from lithium chloride containing brines
US9034294B1 (en) 2009-04-24 2015-05-19 Simbol, Inc. Preparation of lithium carbonate from lithium chloride containing brines
US11649170B2 (en) 2009-04-24 2023-05-16 Terralithium Llc Preparation of lithium carbonate from lithium chloride containing brines
US9834449B2 (en) 2009-04-24 2017-12-05 Alger Alternative Energy, Llc Preparation of lithium carbonate from lithium chloride containing brines
US10773970B2 (en) 2009-04-24 2020-09-15 Terralithium Llc Preparation of lithium carbonate from lithium chloride containing brines
US10829676B2 (en) 2009-04-24 2020-11-10 Terralithium Llc Treated geothermal brine compositions with reduced concentration of silica, iron and lithium
US11466191B2 (en) 2009-04-24 2022-10-11 Terralithium Llc Treated geothermal brine compositions with reduced concentration of silica, iron and lithium
US11828272B2 (en) 2009-06-24 2023-11-28 Terralithium Llc Process for producing geothermal power, selective removal of silica and iron from brines, and improved injectivity of treated brines
US12221671B2 (en) 2009-06-24 2025-02-11 Terralithium Llc Treated geothermal brine compositions with reduced concentrations of silica, iron and manganese
US9051827B1 (en) 2009-09-02 2015-06-09 Simbol Mining Corporation Selective removal of silica from silica containing brines
US9012357B2 (en) 2009-12-18 2015-04-21 Simbol, Inc. Lithium extraction composition and method of preparation thereof
US8637428B1 (en) 2009-12-18 2014-01-28 Simbol Inc. Lithium extraction composition and method of preparation thereof
US9074265B2 (en) 2010-02-17 2015-07-07 Simbol, Inc. Processes for preparing highly pure lithium carbonate and other highly pure lithium containing compounds
US10199665B2 (en) 2014-01-27 2019-02-05 Fuelcell Energy, Inc. Fuel cell matrix composition and method of manufacturing same
US10109869B2 (en) 2014-01-27 2018-10-23 Fuelcell Energy, Inc. Fuel cell matrix composition and method of manufacturing same
WO2015112982A1 (en) * 2014-01-27 2015-07-30 Fuelcell Energy, Inc. Fuel cell matrix composition and method of manufacturing same
US11205795B2 (en) 2016-11-21 2021-12-21 Fuelcell Energy, Inc. Reinforced matrix for molten carbonate fuel cell and method for manufacturing the same
US11431016B2 (en) 2017-04-12 2022-08-30 Fuelcell Energy, Inc. Binder for electrolyte matrix for molten carbonate fuel cells
US10604414B2 (en) 2017-06-15 2020-03-31 Energysource Minerals Llc System and process for recovery of lithium from a geothermal brine
US12227426B2 (en) 2017-06-15 2025-02-18 Iliad Ip Company, Llc Process for recovery of lithium from a geothermal brine
US11904297B1 (en) 2023-01-11 2024-02-20 Iliad Ip Company, Llc Process for manufacturing lithium selective adsorption/separation media

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